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Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery

[Image: see text] Glycosaminoglycan-based hydrogels hold great potential for applications in tissue engineering and regenerative medicine. By mimicking the natural extracellular matrix processes of growth factor binding and release, such hydrogels can be used as a sustained delivery device for growt...

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Autores principales: Newland, Ben, Newland, Heike, Lorenzi, Francesca, Eigel, Dimitri, Welzel, Petra B., Fischer, Dieter, Wang, Wenxin, Freudenberg, Uwe, Rosser, Anne, Werner, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033563/
https://www.ncbi.nlm.nih.gov/pubmed/33754692
http://dx.doi.org/10.1021/acschemneuro.1c00005
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author Newland, Ben
Newland, Heike
Lorenzi, Francesca
Eigel, Dimitri
Welzel, Petra B.
Fischer, Dieter
Wang, Wenxin
Freudenberg, Uwe
Rosser, Anne
Werner, Carsten
author_facet Newland, Ben
Newland, Heike
Lorenzi, Francesca
Eigel, Dimitri
Welzel, Petra B.
Fischer, Dieter
Wang, Wenxin
Freudenberg, Uwe
Rosser, Anne
Werner, Carsten
author_sort Newland, Ben
collection PubMed
description [Image: see text] Glycosaminoglycan-based hydrogels hold great potential for applications in tissue engineering and regenerative medicine. By mimicking the natural extracellular matrix processes of growth factor binding and release, such hydrogels can be used as a sustained delivery device for growth factors. Since neural networks commonly follow well-defined, high-aspect-ratio paths through the central and peripheral nervous system, we sought to create a fiber-like, elongated growth factor delivery system. Cryogels, with networks formed at subzero temperatures, are well-suited for the creation of high-aspect-ratio biomaterials, because they have a macroporous structure making them mechanically robust (for ease of handling) yet soft and highly compressible (for interfacing with brain tissue). Unlike hydrogels, cryogels can be synthesized in advance of their use, stored with ease, and rehydrated quickly to their original shape. Herein, we use solvent-assisted microcontact molding to form sacrificial templates, in which we produced highly porous cryogel microscale scaffolds with a well-defined elongated shape via the photopolymerization of poly(ethylene glycol) diacrylate and maleimide-functionalized heparin. Dissolution of the template yielded cryogels that could load nerve growth factor (NGF) and release it over a period of 2 weeks, causing neurite outgrowth in PC12 cell cultures. This microscale template-assisted synthesis technique allows tight control over the cryogel scaffold dimensions for high reproducibility and ease of injection through fine gauge needles.
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spelling pubmed-80335632021-04-09 Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery Newland, Ben Newland, Heike Lorenzi, Francesca Eigel, Dimitri Welzel, Petra B. Fischer, Dieter Wang, Wenxin Freudenberg, Uwe Rosser, Anne Werner, Carsten ACS Chem Neurosci [Image: see text] Glycosaminoglycan-based hydrogels hold great potential for applications in tissue engineering and regenerative medicine. By mimicking the natural extracellular matrix processes of growth factor binding and release, such hydrogels can be used as a sustained delivery device for growth factors. Since neural networks commonly follow well-defined, high-aspect-ratio paths through the central and peripheral nervous system, we sought to create a fiber-like, elongated growth factor delivery system. Cryogels, with networks formed at subzero temperatures, are well-suited for the creation of high-aspect-ratio biomaterials, because they have a macroporous structure making them mechanically robust (for ease of handling) yet soft and highly compressible (for interfacing with brain tissue). Unlike hydrogels, cryogels can be synthesized in advance of their use, stored with ease, and rehydrated quickly to their original shape. Herein, we use solvent-assisted microcontact molding to form sacrificial templates, in which we produced highly porous cryogel microscale scaffolds with a well-defined elongated shape via the photopolymerization of poly(ethylene glycol) diacrylate and maleimide-functionalized heparin. Dissolution of the template yielded cryogels that could load nerve growth factor (NGF) and release it over a period of 2 weeks, causing neurite outgrowth in PC12 cell cultures. This microscale template-assisted synthesis technique allows tight control over the cryogel scaffold dimensions for high reproducibility and ease of injection through fine gauge needles. American Chemical Society 2021-03-23 /pmc/articles/PMC8033563/ /pubmed/33754692 http://dx.doi.org/10.1021/acschemneuro.1c00005 Text en © 2021 American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Newland, Ben
Newland, Heike
Lorenzi, Francesca
Eigel, Dimitri
Welzel, Petra B.
Fischer, Dieter
Wang, Wenxin
Freudenberg, Uwe
Rosser, Anne
Werner, Carsten
Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery
title Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery
title_full Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery
title_fullStr Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery
title_full_unstemmed Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery
title_short Injectable Glycosaminoglycan-Based Cryogels from Well-Defined Microscale Templates for Local Growth Factor Delivery
title_sort injectable glycosaminoglycan-based cryogels from well-defined microscale templates for local growth factor delivery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033563/
https://www.ncbi.nlm.nih.gov/pubmed/33754692
http://dx.doi.org/10.1021/acschemneuro.1c00005
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